Colon Cancer: Gene >> CENPI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372927
Start	101101155:101101155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85G>A
AA Mutation	p.Ala29Thr(p.A29T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372927
Start	101147785:101147785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761693180
CDS Mutation	c.1849G>A
AA Mutation	p.Ala617Thr(p.A617T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372927
Start	101126719:101126719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.698C>A
AA Mutation	p.Pro233His(p.P233H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372927
Start	101146249:101146249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1798C>A
AA Mutation	p.Leu600Met(p.L600M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372927
Start	101145137:101145137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1639G>A
AA Mutation	p.Ala547Thr(p.A547T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372927
Start	101102391:101102391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344T>G
AA Mutation	p.Ile115Ser(p.I115S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372927
Start	101109554:101109554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446C>T
AA Mutation	p.Ser149Phe(p.S149F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372927
Start	101145143:101145143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752225365
CDS Mutation	c.1645C>T
AA Mutation	p.Arg549Cys(p.R549C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372927
Start	101102313:101102313(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.270delA
AA Mutation	p.Lys90AsnfsTer3(p.K90Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000372927
Start	101127137:101127137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.778-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CENPI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372927
Start	101145144:101145144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1646G>A
AA Mutation	p.Arg549His(p.R549H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript